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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1051543Erstellt: 26. Oktober 2026

Dimethyl Sulfoxide → 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile

https://huagongshe.com/reaction/1051543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
EduktMethyl 1-methyl-1H-benzo[d]imidazole-5-carboxylateHCID 965319—
EduktMethyl 1-methyl-1H-benzo[d]imidazole-6-carboxylateHCID 10583823—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrileHCID 86729302—
Produkt3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrileHCID 8672930338%

Reaktionsschritte

A mixture of CH3CN (0.62 mL, 11.84 mmol), DMSO (2 mL) and NaH (410 mg, 10.26 mmol) was stirred for 45 minutes at room temperature before a solution of methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylate and methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate (1.5 g, 7.89 mmol) in CH3CN (5 mL) was added dropwise. The resulting mixture was stirred at room temperature for 2 h before quenching by the addition of saturated NH4Cl and extraction with DCM (3×30 ml). The combined organic layers were concentrated to give the desired products 3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrile and 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile (600 mg, 38%) and used in the next step without further purification. LCMS (m/z): 200.07 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09388173B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-6b7cda6d52af4946bd6b3c9e33358e99
Quellennotizuspto-grants-2016_07